Canonical Allele Identifier: CA2671177819

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202314-CAGCGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202320_80202325del , CM000666.2:g.80202320_80202325del	GRCh38
NC_000004.11:g.81123474_81123479del , CM000666.1:g.81123474_81123479del	GRCh37
NC_000004.10:g.81342498_81342503del	NCBI36
NG_046725.1:g.22051_22056del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.858_863del MANE Select	ENSP00000406998.2:p.Ser287_Gly288del
ENST00000339711.8:c.858_863del	ENSP00000339764.4:p.Ser287_Gly288del
ENST00000415738.2:c.858_863del	ENSP00000406998.2:p.Ser287_Gly288del
ENST00000504452.5:c.858_863del	ENSP00000423985.1:p.Ser287_Gly288del
ENST00000515013.5:c.858_863del	ENSP00000425149.1:p.Ser287_Gly288del
NM_001099403.1:c.858_863del	NP_001092873.1:p.Ser287_Gly288del
NM_020226.3:c.858_863del	NP_064611.3:p.Ser287_Gly288del
XM_005263144.2:c.861_866del	XP_005263201.1:p.Ser288_Gly289del
XM_005263145.2:c.861_866del	XP_005263202.1:p.Ser288_Gly289del
XM_005263146.3:c.858_863del	XP_005263203.1:p.Ser287_Gly288del
XM_011532133.1:c.1701_1706del	XP_011530435.1:p.Ser568_Gly569del
XM_011532134.1:c.1698_1703del	XP_011530436.1:p.Ser567_Gly568del
XM_011532135.1:c.1560_1565del	XP_011530437.1:p.Ser521_Gly522del
XM_011532136.1:c.1413_1418del	XP_011530438.1:p.Ser472_Gly473del
XM_011532137.1:c.1413_1418del	XP_011530439.1:p.Ser472_Gly473del
XM_011532138.1:c.1413_1418del	XP_011530440.1:p.Ser472_Gly473del
XM_011532139.1:c.1413_1418del	XP_011530441.1:p.Ser472_Gly473del
XM_011532140.1:c.1413_1418del	XP_011530442.1:p.Ser472_Gly473del
XM_011532141.1:c.1275_1280del	XP_011530443.1:p.Ser426_Gly427del
XM_011532142.1:c.1254_1259del	XP_011530444.1:p.Ser419_Gly420del
XM_005263146.4:c.858_863del	XP_005263203.1:p.Ser287_Gly288del
XM_011532133.2:c.1701_1706del	XP_011530435.1:p.Ser568_Gly569del
XM_011532135.2:c.1560_1565del	XP_011530437.1:p.Ser521_Gly522del
XM_011532140.2:c.1413_1418del	XP_011530442.1:p.Ser472_Gly473del
XM_011532141.3:c.1275_1280del	XP_011530443.1:p.Ser426_Gly427del
XM_017008468.1:c.1410_1415del	XP_016863957.1:p.Ser471_Gly472del
XM_017008469.1:c.1497_1502del	XP_016863958.1:p.Ser500_Gly501del
XM_017008470.1:c.1413_1418del	XP_016863959.1:p.Ser472_Gly473del
NM_001099403.2:c.858_863del MANE Select	NP_001092873.1:p.Ser287_Gly288del
NM_020226.4:c.858_863del	NP_064611.3:p.Ser287_Gly288del